78782-06-6 Usage
Description
1,11-Undecanediol, monoacetate is a chemical compound with the molecular formula C14H28O3, derived from undecanediol by the acetylation of one of its hydroxyl groups. This modification endows the compound with unique properties that make it valuable in various industrial applications.
Uses
Used in Lubricant Production:
1,11-Undecanediol, monoacetate is used as an additive in the lubricant industry to enhance the performance and properties of lubricants. Its ability to modify polymers contributes to the improvement of lubricant efficiency and durability.
Used in Plasticizer Manufacturing:
In the plastics industry, 1,11-Undecanediol, monoacetate serves as a component in the production of plasticizers. It helps to increase the flexibility, workability, and durability of plastics, making them more suitable for a wide range of applications.
Used in Surfactant Synthesis:
1,11-Undecanediol, monoacetate is utilized as a chemical intermediate in the synthesis of surfactants. Its properties allow for the creation of surfactants with improved stability and effectiveness in various cleaning and industrial processes.
Used as a Chemical Intermediate:
1,11-Undecanediol, monoacetate is also used as a chemical intermediate in the synthesis of other organic compounds. Its unique structure makes it a valuable building block for the development of new materials and products across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 78782-06-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,8 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78782-06:
(7*7)+(6*8)+(5*7)+(4*8)+(3*2)+(2*0)+(1*6)=176
176 % 10 = 6
So 78782-06-6 is a valid CAS Registry Number.
78782-06-6Relevant articles and documents
Hydroboration. 57. Hydroboration with 9-Borabicyclononane of Alkenes Containing Representative Functional Groups
Brown, Herbert C.,Chen, Jackson C.
, p. 3978 - 3988 (2007/10/02)
The hydroboration of alkenes containing representative functional groups was examined with 9-borabicyclononane (9-BBN) in order to extend the hydroboration reaction for the preparation of functionally substituted organoboranes.Terminal alkenes containing a remote functional group are hydroborated with a remarkable regioselectivity (>=98percent terminal), producing the corresponding stable organoboranes. 9-BBN hydroborates the allylic derivatives so as to place boron essentially on the terminal carbon atom (>=97percent).The directive effect is further enhanced (>=99percent) in the case of β-methylallyl derivatives.The hydroboration of crotyl derivatives attaches boron predominantly at the 2-position, followed by an elimination-rehydroboration sequence.However, crotyl alcohol can be protected against elimination as the tert-butyl or tetrahydropyranyl ethers.The hydroboration-oxidation of ethyl crotonate involves a series of elimination, hydroboration, and condensation processes.In the vinyl, crotyl, and isobutenyl systems, the mesomeric effect of the substituent favors the placement of boron at the β-position, while the inductive effect favors the α-position, with the former effect predominating in most cases.Acyclic β-substituted organoboranes undergo rapid elimination.Nonpolar solvents and lower reaction temperatures decrease the rate of elimination.However, those derived from cyclic vinyl derivatives are relatively stable under neutral conditions, undergoing facile elimination in the presence of a base.
